Canonical Allele Identifier: PA2825613978
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 450485
ClinVar RCV Id: RCV000522128

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Pro1887Leu
CA4475774
NM_001127487.2:c.5660C>T